• 제목/요약/키워드: Methyl ${\alpha}-metylthio-p-isopropoxyphenylacetate$

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An Improved Synthesis of Methyl p-Hydroxyphenylalkanoates

  • Choi, Hong-Dae;Kowak, Yong-Sil;Geum, Dak-Hyun;Son, Byeng-Wha
    • Archives of Pharmacal Research
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    • 제17권3호
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    • pp.190-193
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    • 1994
  • Friedel-Crafts reaction isopropoxybenzene with methyl $\alpha$-chloro-$\alpha$-(maethylthio)acetate 1 afforded methyl $\alpha$-methylthio-p-isopropoxyphenylacetate 2d, which was readily converted into methyl p-isopropoxyphenylacetate 3 by reductive desulfurization with zinc dust in acetic acid. Methylation of 3 with sodium hydride and methyl iodide gave methyl $\alpha$-(p-isopropoxyphenyl)propionate 5. Methyl p-hydroxyphenylakanoates (4,6), useful intermediates for some medicines, were easily prepared by treatment of 3 and 5 with titanium tetrachloride, respectively.

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